Registered Nurse (RN) Research, Clinical Research, FT, Days Prisma HealthRegistered Nurse (RN) Research, Clinical Research, FT, DaysGreenville, South CarolinaProvides patients/families with information regarding clinical trial participation and provides education regarding individual treatment including purpose, potential side effects, and self-care measures, documents interaction. Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.
Research Coordinator II, Administrative Research, Full Time, Days Prisma HealthResearch Coordinator II, Administrative Research, Full Time, DaysGreenville, South CarolinaCoordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines. Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers.
Iach Research Assistant Furman UniversityIach Research AssistantGreenville, SCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
IACH Research Assistant Furman UniversityIACH Research AssistantSCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
Clinical Research Data Coord. Spartanburg Regional Medical CenterClinical Research Data Coord.Spartanburg, SCAttends study team meetings and provides updates to study team members regarding protocol data management activities, including data entry timelines, database locks, unique study requirements, and query management. This position will be responsible for obtaining research data and entering data in the Electronic Data Capture (EDC) for complex interventional therapeutic and supportive care trials including but not limited to industry and cooperative group studies.
Clinical Research Data Coord. Spartanburg Regional Healthcare SystemClinical Research Data Coord.Spartanburg, SCAttends study team meetings and provides updates to study team members regarding protocol data management activities, including data entry timelines, database locks, unique study requirements, and query management. This position will be responsible for obtaining research data and entering data in the Electronic Data Capture (EDC) for complex interventional therapeutic and supportive care trials including but not limited to industry and cooperative group studies.
Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027) Shriners Hospitals for ChildrenClinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)Greenville, South CarolinaWith 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact.
Clinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator IAnderson, South CarolinaTemporaryCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Research Grants Coord. Spartanburg Regional Medical CenterResearch Grants Coord.Batesville, SCPerforms and/or coordinates complex professional duties in the creation and maintenance of restricted fund accounting records, verification, and documentation of restricted fund financial transactions and assists in the preparation and management of restricted account budgets. Responsible for support of financial monitoring and reporting for Upstate Carolina NCI Oncology Research Program (UC-NCORP) grant in accordance with associated Federal guidelines and Institutional policies and procedures.
Research Grants Coord. Spartanburg Regional Healthcare SystemResearch Grants Coord.Greer, SCPerforms and/or coordinates complex professional duties in the creation and maintenance of restricted fund accounting records, verification, and documentation of restricted fund financial transactions and assists in the preparation and management of restricted account budgets. Responsible for support of financial monitoring and reporting for Upstate Carolina NCI Oncology Research Program (UC-NCORP) grant in accordance with associated Federal guidelines and Institutional policies and procedures.
Clinical Research Coordinator I Velocity Clinical Research IncClinical Research Coordinator IAnderson, SCCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Research Coordinator II, Oncology, Full Time, Days Prisma HealthResearch Coordinator II, Oncology, Full Time, DaysGreenville, South CarolinaCoordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines. Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers.
Program Mgr-Non-Sponsored Clinical Research Spartanburg Regional Healthcare SystemProgram Mgr-Non-Sponsored Clinical ResearchSpartanburg, SCThe Manager of Clinical Research Program (Non-Sponsored) works closely with the Director of Clinical Research, Graduate Medical Education (GME) leadership, residency program directors, faculty mentors, Research Compliance, and health system leadership to develop and sustain a scalable model for resident/fellow research and quality improvement support. The manager oversees day-to-day operation of the resident research and QI support program, including workflow coordination, process development, and strategic planning to ensure consistent and high-quality support for resident-fellow scholarly activity and quality improvement work.
Research Development Specialist, General Surgery, Full Time, Days Prisma HealthResearch Development Specialist, General Surgery, Full Time, DaysGreenville, South CarolinaPrepares scientific deliverables such as abstracts, manuscripts, and posters; serves as a liaison among researchers, institutional partners, and project teams; provides education and guidance on research processes and project requirements. Provides specialized research expertise to support residents, fellows, and faculty in the development and execution of research and quality improvement projects that advance the institution’s academic mission.
Financial Transaction Specialist II, Remittance Ops Research Resurgent Capital ServicesFinancial Transaction Specialist II, Remittance Ops ResearchGreenville, South CarolinaThe Financial Transaction Specialist - Remittance Ops Research Specialist II is responsible for assisting internal and external customers with complex payment and reconciliation-oriented tasks. This role requires advanced knowledge of Treasury Operations Remittance Processing processes and systems, sound judgment, and a high level of efficiency and accuracy.
Nurse Practitioner / Physician Assistant - Fellow - Acute Care Surgery - Greenville Prisma HealthNurse Practitioner / Physician Assistant - Fellow - Acute Care Surgery - GreenvilleGreenville, South CarolinaFellowship position for new graduate that has successfully passed the Nurse Practioner or Physician Assistant certification process and is seeking dedicated clinical training within a specific field. Coordinates all medically appropriate clinical pre/post procedure activities, including clinical evaluation and consent, medical histories, and patient care.
NewPhlebotomist/Medical Assistant Life Line ScreeningPhlebotomist/Medical AssistantSpartanburg, SCLife Line Screening works with the nation’s largest pharmaceutical companies and clinical research organizations to assist in patient recruitment for research and development of ground-breaking new treatments and medicines. Must be willing to cross train and perform additional tasks, such as: Ankle Brachial Index, Osteoporosis, AFIB, Patient Registration, and other health screenings within the Medical Assistant position.
Regulatory Coordinator, Heart & Vascular Institute, Full Time, Variable Prisma HealthRegulatory Coordinator, Heart & Vascular Institute, Full Time, VariableGreenville, South CarolinaIn lieu of experience listed above, three (3) years of related experience may be accepted if certified with either Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP) or Master's degree in related field of study. Prepares, submits, and/or assists with multiple levels of research documentation (i.e., Institutional Review Board submissions, educational materials, reports, and study forms).
Medical Assistant I - Atrium Health Rutherford IM FT Advocate Aurora Health IncMedical Assistant I - Atrium Health Rutherford IM FTforest city, NC$22.90–$34.35 / hourCertified or registered as a CMA or RMA by one of the following National Organizations: American Association of Medical Assistants (AAMA), Certified Clinical Medical Assistant (CCMA) certification issued by the National Health Career Association (NHA), RMA certification issued by the American Medical Technologists (AMT), Medical Assistant (NCMA) certification issued by the National Center for Competency Testing (NCCT), Clinical Medical Assistant Certification (CMAC), or American Medical Certification Association (AMCA). Recognized or certified as a CMA or RMA by one of the following National Organizations: American Association of Medical Assistants (AAMA), National Health Career Association (NHA), National Healthcare Worker's Association (NHCWA), National Center for Competency Testing (NCCT), American Registry of Medical Assistants (ARMA) American Medical Technologists (AMT), National Association for Health Professionals (NAHP), National Registry of Medical Assistants (NRMA).
CLINICAL EDUCATION SPECIALIST Greenville County South CarolinaCLINICAL EDUCATION SPECIALISTGreenville, SCObserves field employees on calls and may direct clinical care or operational decisions when necessary; develops and implements various assessment models which evaluate the clinical competency of patient care providers to maintain local credentialing; investigates and reviews medical incidents; represents Clinical Services in the Medical Incident Review Processes; provides resultant remediation; tracks, documents, and reports remedial training progress to the medical director or designee. Evaluates field personnel performance through field observations; conducts remedial training for those EMTs who are identified as in need through simulation, testing, or quality improvement processes; along with the Quality Improvement Specialists, performs retrospective quality review of electronic patient care report data for selected priorities and categories.